A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589636



Internal ID16377045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784710..8816277hg38UCSC Ensembl
Innerchr3:8826396..8857963hg19UCSC Ensembl
Innerchr3:8801396..8832963hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3831568
hg1931568
hg1831568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8214n54
Supporting Variantsnssv1151865, nssv958879, nssv958880, nssv1151866, nssv958881
Samples1780862530_A, HGDP01400
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589636
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer